All of V1739

ID Consequence Gene/Location Detail Geno Type CHD Type
S3660 synonymous_variant NRP1 NM_003873.6:c.1161C>T T/T isolated CHD: TOF
S3661 synonymous_variant NRP1 NM_003873.6:c.1161C>T C/T isolated CHD: TOF
S3662 synonymous_variant NRP1 NM_003873.6:c.1161C>T C/C isolated CHD: TOF
S3663 synonymous_variant NRP1 NM_003873.6:c.1161C>T C isolated CHD: TOF